Date: 15-Aug-2014
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US - Sr. Clinical Research Associate
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· Assists with, attends, and may present at Investigator Meetings for assigned studies.
· Performs study close-out visits.
· Serves as mentor for more junior CRAs as well as new CRAs to the project.
· May conduct field training and assessment of CRA Is and CRA IIs.
· Authorized to request site audits for reasons of validity.
· Performs other duties as requested.
· Strong knowledge of clinical research process and medical terminology.
· At least four years experience in monitoring clinical trials preferred.
· Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
· Excellent organizational and interpersonal skills.
· Ability to interact with all levels of staff to coordinate/execute study activities.
· Ability to handle several priorities within multiple, complex clinical trials.
· Ability to reason independently and recommend specific solutions in clinical settings.
· Able to mentor other CRAs on project team and co-monitor as required.
· Understanding of basic data processing functions, including electronic data capture.
· Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research.
· Able to qualify for a major credit card.
· Valid driver’s license; ability to rent automobile.
· Willingness and ability to travel domestically and internationally, as required.
To apply for this position, please visit
this Website.
Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/